Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 221
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 1992 AND VI 1 AND IP 4
Results: 23
1
2
Dinucleotide repeat polymorphism at the D3S1229 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 290
- By:
- Publication type:
- Article
3
Dinucleotide repeat polymorphism at the D5S356 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 290
- By:
- Publication type:
- Article
4
Dinucleotide repeat polymorphism at the D18S37 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 289
- By:
- Publication type:
- Article
5
Dinucleotide repeat polymorphism at the D21S236 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 289
- By:
- Publication type:
- Article
6
RFLP detected by a genomic probe from the human X-Iinked proteolipid protein gene, PLP.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 288
- By:
- Publication type:
- Article
7
An EcoRI polymorphism for the glutaminyl-tRNA synthetase (QARS) gene on chromosome 1q.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 288
- By:
- Publication type:
- Article
8
Dinucleotide repeat polymorphism at the human erythroid alpha-spectrin (SPTA1) mRNA gene detected using PCR.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 287
- By:
- Publication type:
- Article
9
A further tetranucleotide repeat polymorphism in the vWF gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 287
- By:
- Publication type:
- Article
10
Polymorphism of the CTLA1 gene on chromosome 14.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 286
- By:
- Publication type:
- Article
11
A 19 bp deletion polymorphism adjacent to a dinucleotide repeat polymorphism at the human dopamine β-hydroxylase locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 286
- By:
- Publication type:
- Article
12
Author index.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 291
- Publication type:
- Article
13
Dinucleotide repeat polymorphisms at the P1, HBE1 and MYH7 loci.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 285
- By:
- Publication type:
- Article
14
Identification of a new frameshift mutation and a duplication polymorphism in the CFTR gene in the Algerian population.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 283
- By:
- Publication type:
- Article
15
Skipping of exon 5 as a consequence of the 711 + 1 G→T mutation in the CFTR qene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 281
- By:
- Publication type:
- Article
16
An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new CpG islands of the human X chromosome.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 275
- By:
- Publication type:
- Article
17
Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 229
- By:
- Publication type:
- Article
18
Identification and characterization of a new gene in the human Xq28 region.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 269
- By:
- Publication type:
- Article
19
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 255
- By:
- Publication type:
- Article
20
Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 249
- By:
- Publication type:
- Article
21
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 243
- By:
- Publication type:
- Article
22
A strategy for the selection of transcribed sequences in the Xq28 region.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 235
- By:
- Publication type:
- Article
23
Constraints acting on the exon positions of the splice site sequences and local amino acid composition of the protein.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 4, p. 259
- By:
- Publication type:
- Article